Members of the US Senate at a hearing yesterday expressed skepticism in regard to federal policies limiting the ability of investigators to engage in clinical studies of marijuana’s health benefits.
Senators heard from representatives from the Drug Enforcement Administration (DEA), Food and Drug Administration (FDA), National Institute on Drug Abuse (NIDA), University of Mississippi Medical Center, Arrowhead Regional Medical Center and Project SAM on a variety of issues
The hearing’s most noteworthy moment came when Nora Volkow, director of NIDA, acknowledged that the monopoly on marijuana cultivation for research purposes ought to be amended. Currently, NIDA contracts strictly with the University of Mississippi to grow marijuana for use in research studies. This has led to a cannabis supply that is often delayed significantly and lacking in quality.
Dr. Volkow was supported in her acknowledgement by Dr. Douglas Throckmorton, Deputy Director for the Center for Drug Evaluation and Research with the FDA who answered, “Yes, I think there are advantages to a broad supply of varied marijuana.”
When questioned on whether or not other drugs in the Schedule 1 classification experience this same monopoly, Dr. Volkow said no and there was no scientific reason to treat them differently.
This acknowledgement by Dr. Volkow falls in line with a previous ruling by a DEA administrative law judge in 2007 which was later set aside by former DEA Director, Michele Leonhart.
Other topics discussed at the hearing included expanded access programs which have currently authorized treatment for 400 patients in the U.S. using Epidiolex. Epidiolex is a formulated product containing cannabidiol (CBD) that possesses orphan drug status from the FDA to treat pediatric epilepsy.
While it is clear that Senators Gillibrand (D-NY) and Booker (D-NJ) are making strides to reform federal medical marijuana law, it remains to be seen if Senator Grassley (R-IA), who chairs the Senate Judiciary Committee, and Sen. Feinstein (D-CA) will also take action.